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通过卡托普利封端的钯簇前驱体法制备的用于高效还原4-硝基苯酚的分层结构钯纳米簇催化剂-PdNCs/CoAl(O)/rGO-

Hierarchical-Structured Pd Nanoclusters Catalysts -PdNCs/CoAl(O)/rGO- by the Captopril-Capped Pd Cluster Precursor Method for the Highly Efficient 4-Nitrophenol Reduction.

作者信息

Wang Qinglin, Wei Zhuojun, Li Jin, Feng Danyang, Feng An, Zhang Hui

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, P.O. Box 98, Beijing 100029, China.

出版信息

ACS Appl Mater Interfaces. 2022 Jun 22;14(24):27775-27790. doi: 10.1021/acsami.2c01378. Epub 2022 Jun 9.

Abstract

Water-soluble captopril-capped atomically precise Pd nanoclusters (PdCapt NCs: 1.3 ± 0.5 nm) produced by a simple chemical reduction were supported on preprepared hybrid CoAl-layered double hydroxide/reduced graphene oxide (CoAl-LDH/rGO) by a pH-adjusted electrostatic adsorption strategy followed by proper calcinations, giving a series of novel catalysts -PdNCs/CoAl(O)/rGO- ( (Pd loading) = 0.09, 0.17, 0.43 wt % (ICP), = 230, 250, 280, 300, 320 °C). The characterization results show that the as-obtained catalysts possess the hierarchical nanosheet array morphology. Pd NCs with a size of ∼1.3 to 1.8 nm are highly distributed at the edge sites of the CoAl(O) nanosheets. All of the -PdNCs/CoAl(O)/rGO- catalysts show superior catalytic efficiency for the conversion of 4-nitrophenol to 4-aminophenol, particularly 0.17-PdNCs/CoAl(O)/rGO-300 possesses the highest performance with a turnover frequency (TOF) of 30 042 h, which is the highest among the reported Pd-based catalysts so far. The superior activity of 0.17-PdNCs/CoAl(O)/rGO-300 can be owing to ultrafine Pd NCs with a clean surface, the strongest PdNCs-Co-OH(LDH)-rGO three-phase synergy, and the much improved adsorption of the substrate via π-π stacking upon nanosheet array morphology. Meanwhile, 0.17-PdNCs/CoAl(O)/rGO-300 exhibits excellent catalytic activities for various nitroarenes and anionic azo dyes as well as good reusability with the complete reduction of 4-nitrophenol (4-NP) within 90 s after 10 successive runs. The present work provides not only a simple and convenient strategy for the synthesis of clean, efficient, and environmentally friendly supported metal nanocluster catalysts but also a new idea for the efficient catalytic degradation of environmental pollutants.

摘要

通过简单的化学还原法制备的水溶性卡托普利封端的原子精确钯纳米团簇(PdCapt NCs:1.3±0.5纳米),采用pH调节的静电吸附策略负载在预先制备的杂化钴铝层状双氢氧化物/还原氧化石墨烯(CoAl-LDH/rGO)上,随后进行适当煅烧,得到一系列新型催化剂——PdNCs/CoAl(O)/rGO-((钯负载量)=0.09、0.17、0.43 wt%(电感耦合等离子体质谱法),煅烧温度=230、250、280、300、320℃)。表征结果表明,所制备的催化剂具有分级纳米片阵列形态。尺寸约为1.3至1.8纳米的钯纳米团簇高度分布在CoAl(O)纳米片的边缘位置。所有的-PdNCs/CoAl(O)/rGO-催化剂对4-硝基苯酚转化为4-氨基苯酚均表现出优异的催化效率,特别是0.17-PdNCs/CoAl(O)/rGO-300具有最高的性能,周转频率(TOF)为30042 h⁻¹,这是迄今为止报道的钯基催化剂中最高的。0.17-PdNCs/CoAl(O)/rGO-300的优异活性可能归因于具有清洁表面的超细钯纳米团簇、最强的PdNCs-Co-OH(LDH)-rGO三相协同作用以及通过纳米片阵列形态上的π-π堆积大大改善的底物吸附。同时,0.17-PdNCs/CoAl(O)/rGO-300对各种硝基芳烃和阴离子偶氮染料表现出优异的催化活性,并且在连续10次运行后,90秒内可将4-硝基苯酚(4-NP)完全还原,具有良好的可重复使用性。本工作不仅为合成清洁、高效且环境友好的负载型金属纳米团簇催化剂提供了一种简单便捷的策略,也为环境污染物的高效催化降解提供了新思路。

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